# Beneficial Effects of Long-Lasting Bicarbonate–Sulfate–Calcium–Magnesium Water Intake on Metabolic Dysfunction-Associated Steatotic Liver Disease (MASLD)-Related Outcomes via Impacting Intestinal Permeability (IP), IP-Related Systemic Inflammation, and Oxidative Stress

**Authors:** Marcello Dallio, Mario Romeo, Fiammetta Di Nardo, Giusy Senese, Alessia Silvestrin, Annachiara Coppola, Carmine Napolitano, Paolo Vaia, Claudio Basile, Giuseppina Martinelli, Alessia De Gregorio, Alessandro Federico

PMC · DOI: 10.3390/nu17213452 · 2025-10-31

## TL;DR

Drinking a specific mineral water for a year improved liver disease outcomes by reducing gut permeability and inflammation in patients with MASLD.

## Contribution

This study is the first to demonstrate long-term benefits of mineral water intake on MASLD via effects on intestinal permeability and systemic inflammation.

## Key findings

- Fonte Essenziale® intake significantly reduced intestinal permeability markers and systemic inflammation in MASLD patients.
- Mineral water consumption led to improved liver steatosis and metabolic markers over 12 months.
- Benefits persisted even after a 6-month washout period, suggesting lasting effects.

## Abstract

Background/Objectives: Fonte Essenziale®, a mineral water rich in bicarbonate, sulfate, calcium, and magnesium, has shown potential in modulating the gut–liver axis and microbiota in hepatic steatosis. However, its long-term effects on intestinal permeability (IP), systemic inflammation (SI), and oxidative stress—key factors in Metabolic dysfunction-associated steatotic liver disease (MASLD)—remain unexplored. Methods: Eighty-seven MASLD patients were randomized into two groups: group A received Fonte Essenziale® (400 mL/day, fasting) plus a controlled nutritional regimen for 12 months, followed by a 6-month water washout; group B followed only the controlled nutritional regimen. IP markers, SI (IL-1β, IL-6, TNF-α), oxidative stress (dROMs/BAP), and clinical data (including Controlled Attenuation Parameter—CAP) were assessed at baseline (T0), 12 months (T12), and post-washout (T18). Baseline increased IP (in-IP) was defined by fecal zonulin > 110 ng/mL and serum LBPp > 10 µg/mL; improvement (im-IP) required normalization of both. A ≥30% CAP reduction indicated steatosis improvement. Results: Thirty-eight patients in group A and thirty-nine in group B completed the study. At T12, group A showed significant reductions in fecal zonulin (p: 0.0163) and serum LBPp (p < 0.0001), with increased occludin and claudin 1 (all p < 0.0001). Im-IP prevalence was higher in group A (p: 0.0037). Group A also showed significant reductions in IL-1β, TNF-α, IL-6, LPS, and dROM/BAP (all p < 0.05), especially among those with im-IP. CAP, insulin, and HDL levels improved significantly (all p < 0.0001). Multivariate analysis confirmed water intake (aOR: 2.185, p: 0.001) and im-IP achievement (aHR: 1.267, p: 0.021) as predictors of steatosis improvement. Benefits persisted at T18. Conclusions: Prolonged Fonte Essenziale® intake improved hepatic steatosis and MASLD outcomes by modulating IP, SI, and oxidative stress. This trial has been registered on clinicaltrials.gov (NCT07211113).

## Linked entities

- **Proteins:** si:ch73-61d6.3 (uncharacterized si:ch73-61d6.3), CLDN7 (claudin 7), IL1B (interleukin 1 beta), IL6 (interleukin 6), TNF (tumor necrosis factor), IRF6 (interferon regulatory factor 6)
- **Chemicals:** bicarbonate (PubChem CID 769), sulfate (PubChem CID 1117), calcium (PubChem CID 5460341), magnesium (PubChem CID 5462224)
- **Diseases:** Metabolic dysfunction-associated steatotic liver disease (MONDO:0013209), MASLD (MONDO:0013209)

## Full-text entities

- **Genes:** INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}, OCLN (occludin) [NCBI Gene 100506658] {aka BLCPMG, PPP1R115, PTORCH1}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, CLDN1 (claudin 1) [NCBI Gene 9076] {aka CLD1, ILVASC, SEMP1}, HP (haptoglobin) [NCBI Gene 3240] {aka HP2ALPHA2, HPA1S}, IL1B (interleukin 1 beta) [NCBI Gene 3553] {aka IL-1, IL1-BETA, IL1F2, IL1beta}, LBP (lipopolysaccharide binding protein) [NCBI Gene 3929] {aka BPIFD2}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}
- **Diseases:** MASLD (MESH:D008107), m-IP (MESH:D007410), CAP (OMIM:115650), Inflammation (MESH:D007249), hepatic steatosis (MESH:D005234)
- **Chemicals:** magnesium (MESH:D008274), BAP (-), Calcium (MESH:D002118), water (MESH:D014867), bicarbonate (MESH:D001639), sulfate (MESH:D013431), LPS (MESH:D008070)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12609797/full.md

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Source: https://tomesphere.com/paper/PMC12609797